Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP747587.RABEmL0Olh80Hb51a6F4nGi0_k4S2o4gufRRWR8JviqMo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP747587.RABEmL0Olh80Hb51a6F4nGi0_k4S2o4gufRRWR8JviqMo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP747587.RABEmL0Olh80Hb51a6F4nGi0_k4S2o4gufRRWR8JviqMo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP747587.RABEmL0Olh80Hb51a6F4nGi0_k4S2o4gufRRWR8JviqMo130_provenance.
- NP747587.RABEmL0Olh80Hb51a6F4nGi0_k4S2o4gufRRWR8JviqMo130_assertion description "[Contribution of RET, NTRK3 and EDN3 to the expression of Hirschsprung disease in a multiplex family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP747587.RABEmL0Olh80Hb51a6F4nGi0_k4S2o4gufRRWR8JviqMo130_provenance.
- NP747587.RABEmL0Olh80Hb51a6F4nGi0_k4S2o4gufRRWR8JviqMo130_assertion evidence source_evidence_literature NP747587.RABEmL0Olh80Hb51a6F4nGi0_k4S2o4gufRRWR8JviqMo130_provenance.
- NP747587.RABEmL0Olh80Hb51a6F4nGi0_k4S2o4gufRRWR8JviqMo130_assertion SIO_000772 19556619 NP747587.RABEmL0Olh80Hb51a6F4nGi0_k4S2o4gufRRWR8JviqMo130_provenance.
- NP747587.RABEmL0Olh80Hb51a6F4nGi0_k4S2o4gufRRWR8JviqMo130_assertion wasDerivedFrom befree-2016 NP747587.RABEmL0Olh80Hb51a6F4nGi0_k4S2o4gufRRWR8JviqMo130_provenance.
- NP747587.RABEmL0Olh80Hb51a6F4nGi0_k4S2o4gufRRWR8JviqMo130_assertion wasGeneratedBy ECO_0000203 NP747587.RABEmL0Olh80Hb51a6F4nGi0_k4S2o4gufRRWR8JviqMo130_provenance.
- befree-2016 importedOn "2016-02-19" NP747587.RABEmL0Olh80Hb51a6F4nGi0_k4S2o4gufRRWR8JviqMo130_provenance.